• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/32

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

32 Cards in this Set

  • Front
  • Back

Antidepressants

TCAs, MAOIs, SSRIs, Atypical antidepressants


All equally effective but have different safety and side effects

TCAs

Inhibit reuptake of NE and serotonin, increasing the availability in the synapse


Have increased incidence of SE, require greater monitoring and can be lethal in overdose


Mainstay in treatment of TCA overdose

IV sodium bicarbonate

Side Effects of TCAs

*Anti-HAM


*Hallmark is widened QRS (>100msec)


Antihistaminic-sedation


Antiadrenergic-CV-orthostatic hypotension, tachycardia, arrhythmias,


Anti-muscarinic- dry mouth, constipation, urinary retention, blurred vision, tachycardia


Wt Gain, lethal in overdose


3 C's- Convulsions, coma, cardiotoxicity


Examples of TCAs

Imipramine (tofranil)


Amitryptiline (Elavil)


Trimipramine (Surmontil)


Nortriptyline (Pamelor)- Least to cause orthostatic hypotension


Desipramine (Norpramin)- least sedating, least anticholinergic


Clomipramine (anafranil)- most serotonic specific- OCD


Doxepin (Sinequan)

MAOIs

Prevent inactivation of biogenic amines (NE, Serotonin, dopamine, tyramine)


Very effective for refractory depression and in refractory panic disorder


Side Effects of MAOIs

Common- orthostatic hypotension, drowsiness, wt gain, sexual dysfunction, dry mouth, sleep dysfunction


Serotonin syndrome


Hypertensive crisis- MAOIs are taken with tyramine rich food or sympathomimetics, cause a build up of stored catecholamines

Serotonin syndrome

D/C meds! occurs when SSRIs and MAOIs are taken together


Sx's: lethargy, restlessness, confusion, flushing, diaphoresis, tremor, myoclonic jerks, hyperthermia, hypertonicity, rhabdomyolysis, renal failure, convulsions, coma and death.

Examples of MAOIs

Phenelzine (Nardil)


Tranylcypromine (Parnate)


Iscarboxazid (Marplan)

SSRIs

Inhibit presynaptic serontonin pumps--> increased availability of serotonin in synaptic clefts


low incidence of side effects, no food restrictions, much safer in overdose


Also used to tx some anxiety disorders, OCD and premenstrual dysphoric disorder

Side effects of SSRIs

Low since they don't act on histamine, adrenergic, or muscarinic receptors


Sexual dysfunction


GI


Insomnia


Head ache


Anorexia/weight loss


Serotonin syndrome

Examples of SSRIs

Fluoxetine (Prozac)- longest half life- no need to taper


Sertraline (Zoloft)- increased risk for GI disturbances


Paroxetine (Paxil)- Most serotonin specific- stimulant


Fluvoxamine (Luvox)- only approved for use in OCD


Citalopram (Celexa)


Escitalopram (Lexapro)- fewer side effects, more expensive

SNRIs

Venlafaxine (effexor)- refractory depression, low drug interaction potential, SE's similar to SSRIs, can increase BP

NDRIs

Buproprion (Wellbutrin)- smoking cessation, SAD and adult ADHD, lack of sexual side effects, can exacerbate psychosis, increased risk of seizures

SARIs

Nefazodone (Serzone) and Trazodone (Desyrel)- refractory major depression, major depression with anxiety and insomnia


Side Effects: nausea, dizziness, orthostatic hypotension, cardiac arrhythymias, sedation and priapism

NASAs

Mirtazapine (Remeron)- refractory major depression (especially in patients that need to gain weight)


SE: sedation, weight gain, dizziness, somnolence, tremor, agranulocytosis

Antipsychotics

Traditional- classified according to potency; work by blocking dopamine receptors


Atypical- block both dopamine and serotonin receptors- effect on dopamine is weaker so lower side effects

Traditional antipsychotics-low potency

Have lower affinity for dopamine receptors, higher dose required


Chlorpromazine (thorazine)


Thioridazine (Mellaril)


Increased incidences of anticholinergic and antihistaminic SE


Decreased incidences of extrapyramidal SE and NMS

Traditional antipsychotics- high potency

Greater affinity for dopamine receptors, low dose needed


Haloperidol (Haldol)- LA available- IM x 4-5 weeks


Fluprienazine (Prolixin)- LA available- IM x 2-3 weeks


Trifluoperazine (Stelazine)


Perphenazine (Trilafon)


Pimozide (Orap)


Increased incidences of EPSE's and NMS


Side Effects of Traditional Antipsychotics

1. Antidopaminergic- EPSE, hyperprolactinemia. Tx- decrease dose and administer anti meds


2. Anti-HAM effects


3. Weight gain


4. Increased liver enzymes


5. Ophthalamogic problems


6. Derm problems- rash and photosensitivity


7. Seizures


8. Tardive dyskinesia- writhing of mouth and tongue in patients that have used neuroleptics for > 6 mo (mostly increased in female)


9. NMS- MC in males early in tx, emergency, FALTER (fever, autonomic instability, leukocytosis, tremor, increase CPK, rigidity)

Atypical Antipsychotics

More effective in treating negative symptoms (so 1st line of treatment of schizophrenia


Clozapine (clozaril)- patients must have wkly WBCs to check for agranulocytosis


Risperidone (Risperdal)


Quetiapine (Seroquel)- may cause cataracts so slit lamp exam every 6 mo


Olanzapine (Zyprexa)- hyperlipidemia, glucose intolerance, wt gain, liver toxicity


Ziprasidone (geodon)


Side effects-some anti-HAM

Mood stabilizers

Used to tx acute mania and prevent relapses of manic episodes


Less commonly- major depression, schizophrenia, enhancement of alcohol abstinence, tx of agg or impulsivity

Lithium

Exact MOA is unknown, lithium is secreted by the kidney and OA takes 5-7 days


Therapeutic range- 0.7-1.2, toxic >1.5, lethal 2.0


Side effects: fine tremor, sedation, ataxia, thirst, metallic taste, polyuria, edema, wt gain, GI problems, leukocytosis, thyroid enlargement, hypothyroidism, nephrogenic DI

Factors that affect Lithium levels

NSAIDs (decrease)


Aspirin


Dehydration (increase)


Salt deprivation (increase)


Diuretics


Impaired renal function

Carbamazepine (Tegretol)

especially useful in treatment of mixed episodes and rapid-cycling bipolar, blocks Na+ channels and inhibits action potentials


OA- 5-7 days


Side effects: rash, drowsiness, ataxia, slurred speech, leukopenia, hyponatremia, aplastic anemia, agranulocytosis, teratogenic (neural tube defects)

Valproic acid (Depakene)

Mixed manic and rapid cycling, increased CNS levels of GABA


Side effects: sedation, wt gain, alopecia, hemorrhagic, pancreatitis, hepatoxicity, thrombocytopenia, neural tube defect

Anxiolytics/hypnotics

depress the CNS


Indications: anxiety, muscle spasms, seizures, sleep disorders, alcohol withdrawal, anesthesia induction

Benzodiazepine

First line treatment


Safety at high doses, but have potential for tolerance and dependence after prolonged use


Potentiate the effects of GABA


Side effects- Drowsiness, mental impairment, low motor coordination

Long acting BDZ

1-3 days


Chlordiazepoxide


Diazepem (Valium)- rapid onset- anxiety and seizure control


Intermediate Acting BDZ

10-20 hours


Alprazolam (xanax)- panic attacks


Clonazepam (Klonopin)- panic attacks, anxiety


Lorazepam (Ativan)- tx of panic attacks, alcohol withdrawal


Temazepam (Restoril)- tx of insomnia

Short acting BDZ

3-8 hours


Oxazepam (Serax)


Triazolam (Halcion)- rapid onset, insomnia

Buspirone (Buspar)

Alternative to BDZ or venlafaxine for tx of GAD, slower OA (1-2 wks)


Anxiolytic action is at 5HT-1A receptor


doesn't potentiate CNS depression of ETOH